Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-13T04:57:51.897Z Has data issue: false hasContentIssue false

Allium vegetables intake and endometrial cancer risk

Published online by Cambridge University Press:  01 September 2009

Carlotta Galeone*
Affiliation:
Istituto di Ricerche Farmacologiche ‘Mario Negri’, Via La Masa 19, I-20156 Milan, Italy Istituto di Statistica Medica e Biometria ‘G.A. Maccacaro’, Università degli Studi di Milano, Milan, Italy
Claudio Pelucchi
Affiliation:
Istituto di Ricerche Farmacologiche ‘Mario Negri’, Via La Masa 19, I-20156 Milan, Italy
Luigino Dal Maso
Affiliation:
Unità di Epidemiologia e Biostatistica, IRCCS Centro di Riferimento Oncologico di Aviano, Aviano (Pordenone), Italy
Eva Negri
Affiliation:
Istituto di Ricerche Farmacologiche ‘Mario Negri’, Via La Masa 19, I-20156 Milan, Italy
Maurizio Montella
Affiliation:
Servizio di Epidemiologia, Istituto Tumori ‘Fondazione Pascale’, Naples, Italy
Antonella Zucchetto
Affiliation:
Unità di Epidemiologia e Biostatistica, IRCCS Centro di Riferimento Oncologico di Aviano, Aviano (Pordenone), Italy
Renato Talamini
Affiliation:
Unità di Epidemiologia e Biostatistica, IRCCS Centro di Riferimento Oncologico di Aviano, Aviano (Pordenone), Italy
Carlo La Vecchia
Affiliation:
Istituto di Ricerche Farmacologiche ‘Mario Negri’, Via La Masa 19, I-20156 Milan, Italy Istituto di Statistica Medica e Biometria ‘G.A. Maccacaro’, Università degli Studi di Milano, Milan, Italy
*
Corresponding author: Email galeone@marionegri.it
Rights & Permissions [Opens in a new window]

Abstract

Objective

The potential role of allium vegetables on endometrial cancer risk has been scarcely investigated and the results of previous Chinese studies are not easily applicable to Western populations. Therefore, we evaluated the relationship between onion and garlic intake and endometrial cancer, using data from an Italian case–control study.

Setting

We analysed data from a multi-centre case–control study of 454 endometrial cancer cases and 908 controls, admitted to the same hospitals for a wide spectrum of acute, non-neoplastic conditions. Information was collected by trained interviewers using a validated and reproducible FFQ. Multivariate odds ratios and 95 % confidence intervals were obtained after allowance for recognized confounding factors.

Results

Compared with non-users, the OR of endometrial cancer for successive categories of onion intake were 0·94 (95 % CI 0·72, 1·21) for <2 portions/week and 0·40 (95 % CI 0·22, 0·72) for ≥2 portions/week, with a significant inverse trend in risk (P = 0·01). The OR for an increment of one portion (i.e. 80 g) of onions per week was 0·81 (95 % CI 0·70, 0·95). For garlic, the OR for successive categories of intake were 0·89 (95 % CI 0·68, 1·15) for intermediate use and 0·62 (95 % CI 0·42, 0·92) for high use, with a significant inverse trend in risk (P = 0·02).

Conclusions

Our study found a moderate protective role of allium vegetables on the risk of endometrial cancer.

Type
Short communication
Copyright
Copyright © The Authors 2008

Several epidemiological studies have found that diet may influence endometrial cancer independently from obesity, which is an established risk factor that acts by increasing oestrogen(Reference Cook, Weiss, Doherty and Chen1, Reference Salazar-Martinez, Lazcano-Ponce, Lira-Lira, Escudero-De los Rios, Salmeron-Castro, Larrea and Hernandez-Avila2). However, the evidence for the role of specific foods or food groups is limited and controversial(Reference Cook, Weiss, Doherty and Chen1). Several investigations reported an inverse relationship with vegetables and fruit intake, but these findings are not consistent(Reference Shu, Zheng, Potischman, Brinton, Hatch, Gao and Fraumeni3Reference Littman, Beresford and White6). To our knowledge, the potential role of allium vegetables on endometrial cancer risk has been investigated in only two case–control studies among Chinese women in Shanghai(Reference Shu, Zheng, Potischman, Brinton, Hatch, Gao and Fraumeni3, Reference Tao, Xu, Zheng, Gao, Ruan, Cheng, Xiang and Shu4). The first study was conducted among 268 cases and 268 controls and found a moderate non-significant inverse association between allium vegetables intake and endometrial cancer risk(Reference Shu, Zheng, Potischman, Brinton, Hatch, Gao and Fraumeni3). The second study was conducted among 832 cases and 846 controls and found an OR of 0·76 (95 % CI 0·56, 1·03) for the highest v. the lowest quartile of allium vegetables intake, with a significant trend in risk (P = 0·04)(Reference Tao, Xu, Zheng, Gao, Ruan, Cheng, Xiang and Shu4). The inverse association was appreciably stronger in premenopausal women, with an OR of 0·41 (95 % CI 0·24, 0·71) for the highest v. the lowest quartile of intake (P < 0·01).

The results of these studies are not easily applicable to Western populations, whose dietary habits are largely different and in particular whose garlic intake is far lower(Reference Galeone, Pelucchi, Levi, Negri, Franceschi, Talamini, Giacosa and La Vecchia7). Therefore, we evaluated the relationship between onion and garlic intake and endometrial cancer, using data from a multi-centre case–control study conducted in Italy.

Materials and methods

A case–control study on endometrial cancer was conducted between 1992 and 2006 in three Italian areas, including greater Milan, the provinces of Udine and Pordenone in northern Italy and the urban area of Naples in southern Italy. Cases were 454 women (median age 60 years, range 18–79 years) with incident, histologically confirmed endometrial cancer (code 182.0 in the International Classification of Diseases, 9th revision), admitted to major teaching and general hospitals of the study areas. Controls were 908 women (median age 61 years, range 19–80 years) admitted to the same hospitals as cases for a wide spectrum of acute non-neoplastic conditions. Controls were matched with cases by quinquennia of age and study centre, with a case to control ratio of 1:2. Thirty-six per cent of controls were admitted for traumas, 32 % for other orthopaedic disorders, 9 % for acute surgical conditions and 23 % for miscellaneous other illnesses, including eye, nose, ear, skin or dental disorders.

Interviewers used a structured questionnaire to gather information on sociodemographic factors, anthropometric variables, smoking, alcohol and other lifestyle habits, problem-oriented medical history, physical activity and history of cancer in first-degree relatives. Information on diet referred to the 2 years preceding diagnosis and was based on an FFQ that had previously been tested for reproducibility and validity(Reference Decarli, Franceschi, Ferraroni, Gnagnarella, Parpinel, La Vecchia, Negri, Salvini, Falcini and Giacosa8, Reference Franceschi, Negri and Salvini9). The FFQ included seventy-eight foods, food groups or recipes, and allowed an estimation of energy intake. Among the items in the FFQ, two questions referred specifically to the consumption of onion and garlic. For onion intake, we asked for the weekly frequency of consumption and usual portion size (small, intermediate, large), where an intermediate portion corresponded to 80 g of onion. A small portion was considered as 0·7 times an intermediate portion, and a large portion was considered as 1·3 times an intermediate portion. Frequencies of less than once per week, but at least once per month, were coded as 0·5 per week. For frequency of garlic use, we asked for the common consumption as a qualitative variable, scored as 1 for non-use or low use, 2 for intermediate use and 3 for high use. No additional information on the type of garlic and onion consumed or on manner of use (fresh, powders or garlic supplements) was available.

To compare cases and controls according to selected anthropometric and dietary variables, we used a two-sided χ 2 test for categorical variables, a two-sided Student’s t test for approximately normally distributed variables (based on the Shapiro–Wilk statistic) and a two-sided Wilcoxon’s rank-sum test otherwise.

The odds ratio and the corresponding 95 % confidence intervals for different levels of onion intake (non-users; infrequent users, >0 to <2 portions/week; frequent users, ≥2 portions/week) and garlic use (none or low, intermediate, high) were derived using multiple logistic regression models stratified for study centre and quinquennia of age, and adjusted for years of education, total energy intake, BMI, age at menarche, parity, oral contraceptive and hormone replacement therapy use, and menopausal status(Reference Breslow and Day10).

Results

Table 1 shows the distribution of 454 cases of endometrial cancer and 908 controls according to age, personal and lifestyle characteristics and selected dietary factors. BMI and energy intake of cases were higher than those of controls (P < 0·0001 and P = 0·015, respectively). Cases consumed total vegetables, onions and garlic less frequently than controls, even if these differences were not statistically significant.

Table 1 Frequency distribution of 454 endometrial cancer cases and 908 controls according to relevant covariates and information on selected dietary aspects, Italy, 1992–2006

*Calculated using the χ 2 test for education, age at menarche, parity, oral contraceptive use, hormone replacement therapy use and menopausal status; the two-sided Student’s t test for BMI and energy intake; and the two-sided Wilcoxon rank-sum test for other variables.

†Sum did not equal total because of some missing values.

Table 2 reports the distribution of endometrial cancer cases and controls, the OR and 95 % CI for successive levels of onion intake and garlic use. Compared with non-users, the crude OR of endometrial cancer cases for successive categories of onion intake were 0·99 (95 % CI 0·78, 1·26) for <2 portions/week and 0·56 (95 % CI 0·33, 0·93) for ≥2 portions/week. The corresponding multivariate OR were 0·94 (95 % CI 0·72, 1·21) and 0·40 (95 % CI 0·22, 0·72), with a significant inverse trend in risk (P = 0·01). The multivariate OR for an increment of one portion of onions per week (i.e. 80 g/week) was 0·81 (95 % CI 0·70, 0·95). For garlic, the crude OR for successive categories of intake were 0·98 (95 % CI 0·78, 1·24) for intermediate use and 0·73 (95 % CI 0·51, 1·02) for high use, as compared with non-/low users. The corresponding multivariate OR were 0·89 (95 % CI 0·68, 1·15) and 0·62 (95 % CI 0·42, 0·92), with a significant inverse trend in risk (P = 0·02). We also considered the OR in separate strata of age, education, BMI and, for garlic, intake of lipids, proteins and cruciferous vegetables. No significant heterogeneity emerged across any of the strata considered (data not shown).

Table 2 Distribution of 454 endometrial cancer cases and 908 controls and odds ratiosFootnote * and 95 % confidence intervals according to onion intake (portions/week) and garlic use, Italy, 1992–2006

* Estimates from logistic regression, stratified for age and centre, and adjusted for total energy intake, education, BMI, age at menarche, parity, oral contraceptive use, hormone replacement therapy use and menopausal status.

OR for an increment of one portion (80 g) per week.

The sum does not add up to the total because of some missing values. §Reference category.

Discussion

Epidemiological studies suggest that allium vegetable intake reduces the risk of cancer and laboratory investigations have provided convincing evidence that selected substances contained in garlic and other allium vegetables inhibit a variety of chemically induced tumours in animals(Reference Galeone, Pelucchi, Levi, Negri, Franceschi, Talamini, Giacosa and La Vecchia7, Reference Fleischauer and Arab11, Reference Nakagawa, Tsuta, Kiuchi, Senzaki, Tanaka, Hioki and Tsubura12). The protective effect appears to be related to the presence of organosulfur compounds, mainly allyl derivates, which inhibit proliferation of human digestive tract, mammary, endometrial and colon cancer cells(Reference Fleischauer and Arab11, Reference Hirsch, Danilenko, Giat, Miron, Rabinkov, Wilchek, Mirelman, Levy and Sharoni13). Although the exact preventive mechanisms on cancer are not clear, several hypotheses have been proposed. These include modulation of the activity of several metabolizing enzymes that activate and detoxify carcinogens and inhibit DNA adduct formation, antioxidant and free radicals scavenging properties, and regulation of cell proliferation, apoptosis and immune responses(Reference Shukla and Kalra14). Moreover, several studies have reported the antihypertensive effect of garlic(Reference Banerjee and Maulik15), and hypertension has been directly associated with endometrial cancer risk(Reference Cook, Weiss, Doherty and Chen1, Reference Soler, Chatenoud, Negri, Parazzini, Franceschi and La Vecchia16).

However, onion and garlic intake in Italy could also be simply considered markers of a healthier lifestyle, which may include complex aspects of quantity and quality of the diet, and in particular of a diet rich in vegetables that has been inversely associated with endometrial cancer(Reference Bravi, Scotti and Bosetti17). In fact, in the Italian diet, onion and garlic are often eaten or cooked in combination with other foods, such as tomatoes and olive oil in salads and tomato sauces for pasta.

Among the limitations of the present study, selection and recall biases are possible. A recent cancer diagnosis might have influenced recall of diet for cases, although awareness of dietary hypotheses for endometrial cancer is limited among the general population and the interviewers. Further, by interviewing subjects in the same hospital setting, the comparability of information between cases and controls is improved(Reference D’Avanzo, La Vecchia, Katsouyanni, Negri and Trichopoulos18). Patients hospitalized for chronic or digestive tract conditions were excluded. We collected no information on the variety of onions and type of garlic used and on modalities of cooking; nor on the intake of other allium vegetables, such as scallions and chives, which were inversely related to endometrial cancer risk in a Chinese study(Reference Tao, Xu, Zheng, Gao, Ruan, Cheng, Xiang and Shu4, Reference Yang, Meyers, van der Heide and Liu19); nor on genetic polymorphisms that may be involved in endometrial cancer.

Major strengths of the present study are its large size combined with the collection of extensive dietary information using a satisfactorily reproducible and valid FFQ(Reference Decarli, Franceschi, Ferraroni, Gnagnarella, Parpinel, La Vecchia, Negri, Salvini, Falcini and Giacosa8, Reference Franceschi, Negri and Salvini9), the comparable catchment areas of cases and controls, the high participation rate and the possibility of allowance for intake of energy and for several covariates in the analyses. Thus, we were able to allow in the analysis for selected major lifestyle and nutritional factors, including physical activity, vegetable and fruit consumption, but the multivariate OR were not appreciably modified. The Spearman correlation coefficient for reproducibility of frequency of onion intake was 0·48, and the concordance of the subjective question on garlic use was highly reproducible in 70–80 % of the subjects(Reference Franceschi, Negri and Salvini9).

Our study, the first from a Western country, found a moderate protective role of allium vegetables on the risk of endometrial cancer, supporting previous findings reported among Chinese populations.

Acknowledgements

The authors thank Mrs I. Garimoldi for editorial assistance. The work was conducted with the contribution of the Italian Association for Cancer Research (AIRC), the Italian League Against Cancer and the Italian Ministry of Research (PRIN 2005). The work in this paper was undertaken while C.L.V. was a senior fellow at the International Agency for Research on Cancer. The authors had no conflicts of interest. C.G. and C.L.V. had the original idea for the study and wrote the report. C.G. and C.P. analysed the data. A.Z. assisted in data checking and analysis. L.D.M., E.N. and M.M. organized data collection in different study centres. C.L.V., E.N. and R.T. conceived and coordinated the studies. All authors revised and approved the manuscript.

References

1.Cook, LS, Weiss, NS, Doherty, JA & Chen, C (2006) Endometrial cancer. In Cancer Epidemiology and Prevention, 3rd ed, pp. 10271043 [D Schottenfeld and JF Fraumeni, editors]. New York: Oxford University Press.CrossRefGoogle Scholar
2.Salazar-Martinez, E, Lazcano-Ponce, EC, Lira-Lira, GG, Escudero-De los Rios, P, Salmeron-Castro, J, Larrea, F & Hernandez-Avila, M (2000) Case–control study of diabetes, obesity, physical activity and risk of endometrial cancer among Mexican women. Cancer Causes Control 11, 707711.CrossRefGoogle ScholarPubMed
3.Shu, XO, Zheng, W, Potischman, N, Brinton, LA, Hatch, MC, Gao, YT & Fraumeni, JF Jr (1993) A population-based case–control study of dietary factors and endometrial cancer in Shanghai, People’s Republic of China. Am J Epidemiol 137, 155165.CrossRefGoogle ScholarPubMed
4.Tao, MH, Xu, WH, Zheng, W, Gao, YT, Ruan, ZX, Cheng, JR, Xiang, YB & Shu, XO (2005) A case–control study in Shanghai of fruit and vegetable intake and endometrial cancer. Br J Cancer 92, 20592064.CrossRefGoogle ScholarPubMed
5.Tzonou, A, Lipworth, L, Kalandidi, A, Trichopoulou, A, Gamatsi, I, Hsieh, CC, Notara, V & Trichopoulos, D (1996) Dietary factors and the risk of endometrial cancer: a case–control study in Greece. Br J Cancer 73, 12841290.CrossRefGoogle ScholarPubMed
6.Littman, AJ, Beresford, SA & White, E (2001) The association of dietary fat and plant foods with endometrial cancer (United States). Cancer Causes Control 12, 691702.CrossRefGoogle ScholarPubMed
7.Galeone, C, Pelucchi, C, Levi, F, Negri, E, Franceschi, S, Talamini, R, Giacosa, A & La Vecchia, C (2006) Onion and garlic use and human cancer. Am J Clin Nutr 84, 10271032.CrossRefGoogle ScholarPubMed
8.Decarli, A, Franceschi, S, Ferraroni, M, Gnagnarella, P, Parpinel, MT, La Vecchia, C, Negri, E, Salvini, S, Falcini, F & Giacosa, A (1996) Validation of a food-frequency questionnaire to assess dietary intakes in cancer studies in Italy. Results for specific nutrients. Ann Epidemiol 6, 110118.CrossRefGoogle ScholarPubMed
9.Franceschi, S, Negri, E, Salvini, S et al. (1993) Reproducibility of an Italian food frequency questionnaire for cancer studies: results for specific food items. Eur J Cancer 29A, 22982305.CrossRefGoogle ScholarPubMed
10.Breslow, NE & Day, NE (1980) Statistical Methods in Cancer Research. vol. 1: The Analysis of Case–Control Studies. IARC Science Publication no. 32. Lyon: International Agency for Research on Cancer.Google Scholar
11.Fleischauer, AT & Arab, L (2001) Garlic and cancer: a critical review of the epidemiologic literature. J Nutr 131, 1032S1040S.CrossRefGoogle Scholar
12.Nakagawa, H, Tsuta, K, Kiuchi, K, Senzaki, H, Tanaka, K, Hioki, K & Tsubura, A (2001) Growth inhibitory effects of diallyl disulfide on human breast cancer cell lines. Carcinogenesis 22, 891897.CrossRefGoogle ScholarPubMed
13.Hirsch, K, Danilenko, M, Giat, J, Miron, T, Rabinkov, A, Wilchek, M, Mirelman, D, Levy, J & Sharoni, Y (2000) Effect of purified allicin, the major ingredient of freshly crushed garlic, on cancer cell proliferation. Nutr Cancer 38, 245254.CrossRefGoogle ScholarPubMed
14.Shukla, Y & Kalra, N (2007) Cancer chemoprevention with garlic and its constituents. Cancer Lett 247, 167181.CrossRefGoogle ScholarPubMed
15.Banerjee, SK & Maulik, SK (2002) Effect of garlic on cardiovascular disorders: a review. Nutr J 1, 4.CrossRefGoogle ScholarPubMed
16.Soler, M, Chatenoud, L, Negri, E, Parazzini, F, Franceschi, S & La Vecchia, C (1999) Hypertension and hormone-related neoplasms in women. Hypertension 34, 320325.CrossRefGoogle ScholarPubMed
17.Bravi, F, Scotti, L, Bosetti, C et al. (2008) Foods groups and endometrial cancer risk: a case–control study. Am J Obset Gynecol (In the Press).Google ScholarPubMed
18.D’Avanzo, B, La Vecchia, C, Katsouyanni, K, Negri, E & Trichopoulos, D (1997) An assessment, and reproducibility of food frequency data provided by hospital controls. Eur J Cancer Prev 6, 288293.CrossRefGoogle ScholarPubMed
19.Yang, J, Meyers, KJ, van der Heide, J & Liu, RH (2004) Varietal differences in phenolic content and antioxidant and antiproliferative activities of onions. J Agric Food Chem 52, 67876793.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Frequency distribution of 454 endometrial cancer cases and 908 controls according to relevant covariates and information on selected dietary aspects, Italy, 1992–2006

Figure 1

Table 2 Distribution of 454 endometrial cancer cases and 908 controls and odds ratios* and 95 % confidence intervals according to onion intake (portions/week) and garlic use, Italy, 1992–2006